A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043299



Internal ID96576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10864755..10869291hg38UCSC Ensembl
chr11:10886302..10890838hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg384537
hg194537
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497585
Supporting Variants
Samples
Known GenesZBED5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043299
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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